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Toxins and Antibiotic Resistance in Staphylococcus aureus Isolated from a Major Hospital in Lebanon
Author(s) -
Sima Tokajian,
Dominik Haddad,
Rana Andraos,
Fuad Hashwa,
George F. Araj
Publication year - 2011
Publication title -
isrn microbiology
Language(s) - English
Resource type - Journals
eISSN - 2090-7486
pISSN - 2090-7478
DOI - 10.5402/2011/812049
Subject(s) - staphylococcus aureus , microbiology and biotechnology , virulence , biology , antibiotic resistance , drug resistance , restriction fragment length polymorphism , 23s ribosomal rna , typing , antibiotics , phage typing , molecular epidemiology , staphylococcal infections , polymerase chain reaction , virology , gene , bacteria , genetics , genotype , ribosome , rna
Molecular characterization of Staphylococcus aureus is of both clinical and infection control importance. Virulence determinants using PCR and multiple drug resistance profiles were studied in 130 S. aureus isolates. PCR-RFLP analysis of the 16S–23S DNA spacer region was done to investigate the level of 16S–23S ITS (internal transcribed spacer) polymorphism. Methicillin-resistant S. aureus (MRSA), which represented 72% of the studied isolates, showed multiple drug resistance with 18% being resistant to 10–18 of the drugs used compared to a maximum resistance to 9 antibiotics with the methicillin sensitive S. aureus (MSSA) isolates. Exfoliative toxin A (ETA) was more prevalent than B (ETB) with virulent determinants being additionally detected in multiple drug-resistant isolates. 16S–23S ITS PCR-RFLP combined with sequencing of the primary product was successful in generating molecular fingerprints of S. aureus and could be used for preliminary typing. This is the first study to demonstrate the incidence of virulent genes, ACME, and genetic diversity of S. aureus isolates in Lebanon. The data presented here epitomize a starting point defining the major genetic populations of both MRSA and MSSA in Lebanon and provide a basis for clinical epidemiological studies.

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